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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv7097097copy number variation1nstd102humanUncertain significance GRCh37 chr6: 84,765,038-86,267,798 , GRCh38.p12 chr6: 84,055,319-85,558,080 MRAP2, LOC107986619, 18 more genes
    nsv7052601inversion1nstd229human GRCh38 chr6: 85,122,647-85,919,414 , GRCh37.p13 chr6: 85,832,365-86,629,132 NT5E, SNORD50A, 18 more genes
    nsv7043869inversion1nstd229human GRCh38 chr6: 85,210,624-85,567,280 , GRCh37.p13 chr6: 85,920,342-86,276,998 RPL31P32, TPT1P6, 7 more genes
    nsv6805275copy number variation1nstd229human GRCh38 chr6: 85,284,738-85,590,427 , GRCh37.p13 chr6: 85,994,456-86,300,145 SNX14, NT5E, 6 more genes
    nsv6804375copy number variation1nstd229human GRCh38 chr6: 85,391,856-85,404,916 , GRCh37.p13 chr6: 86,101,574-86,114,634 LINC02535
    nsv6798390copy number variation1nstd229human GRCh38 chr6: 84,932,542-85,530,791 , GRCh37.p13 chr6: 85,642,260-86,240,509 RPL31P32, LINC02535, 9 more genes
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6636656copy number variation1nstd102humanUncertain significance GRCh37 chr6: 86,098,133-88,663,964 , GRCh38.p12 chr6: 85,388,415-87,954,246 LINC02535, RPL7P27, 45 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6562641inversion1nstd223human GRCh38 chr6: 84,595,873-85,427,122 , GRCh37.p13 chr6: 85,305,591-86,136,840 LOC100421093, LOC100421583, 9 more genes
    nsv6412928copy number variation1nstd223human GRCh38 chr6: 84,932,542-85,530,787 , GRCh37.p13 chr6: 85,642,260-86,240,505 NT5E, KRT18P30, 9 more genes
    nsv6410592copy number variation1nstd223human GRCh38 chr6: 85,391,855-85,404,915 , GRCh37.p13 chr6: 86,101,573-86,114,633 LINC02535
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6290989copy number variation1nstd102humanPathogenic GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748 KRT18P30, LOC107986620, 58 more genes
    nsv5463851copy number variation1nstd206human GRCh38 chr6: 85,334,000-85,428,261 , GRCh37.p13 chr6: 86,043,718-86,137,979 TPT1P6, LINC02535, 1 more genes
    nsv5369383translocation1nstd200human GRCh38 chr6: 85,390,944-85,390,944 , GRCh38 chr6: 85,391,009-85,391,009 , GRCh37.p13 chr6: 86,100,727-86,100,727 , GRCh37.p13 chr6: 86,100,662-86,100,662 LINC02535
    nsv5116030mobile element insertion1nstd203human GRCh38 chr6: 85,388,113-85,388,128 , GRCh37.p13 chr6: 86,097,831-86,097,846 LINC02535
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv5037999inversion1nstd200human GRCh38 chr6: 85,122,647-85,919,417 , GRCh37.p13 chr6: 85,832,365-86,629,135 , LOC100127917, 19 more genes
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